SDHD公司
SDHB系统
SDHA
副神经节瘤
外显率
医学
耳鼻咽喉科
遗传咨询
嗜铬细胞瘤
疾病
基因检测
生物信息学
内科学
突变
病理
表型
琥珀酸脱氢酶
遗传学
基因
生物
外科
种系突变
线粒体
作者
Nathan D. Cass,Melissa A. Schopper,Jonathan A. Lubin,Lauren Fishbein,Samuel P. Gubbels
标识
DOI:10.1177/0003489420931540
摘要
BACKGROUND: Recommendations regarding head and neck paragangliomas (HNPGL) have undergone a fundamental reorientation in the last decade as a result of increased understanding of the genetic and pathophysiologic basis of these disorders. OBJECTIVE: We aim to provide an overview of HNPGL and recent discoveries regarding their molecular genetics, along with updated recommendations on workup, treatment, and surveillance, and their implications for otolaryngologists treating patients with these disorders. RESULTS: mutations require frequent biochemical screening and whole-body imaging, as well as lifelong follow-up with an expert in hereditary pheochromocytoma and paraganglioma syndromes. CONCLUSION: Otolaryngologists are likely to encounter patients with HNPGL. Keeping abreast of the latest recommendations, especially regarding genetic testing, workup for additional tumors, multi-disciplinary approach to care, and need for lifelong surveillance, will help otolaryngologists appropriately care for these patients.
科研通智能强力驱动
Strongly Powered by AbleSci AI